NDC 67296-0559
Metformin Hydrochloride 500 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-008.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it and relabels it
Recalls
- Feb 2, 2018 · Class III · Aurobindo Pharma Ltd.
Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of Metformin HCl 1000mg
Lots: Lot#: MTSC17145-A, Exp. July 2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet
- Strength
- 500 mg
- Approval
- ANDA ANDA077095
- On the market since
- Jan 14, 2005
- Package NDCs
67296-0559-167296-0559-367296-0559-9- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2005
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